Title of article
Effect of Albendazole on Tau and Stathmin Expression in Metastatic Breast Cancer
Author/Authors
Javdan ، Sepideh Department of Biochemistry - Faculty Biology - Islamic Azad University, Falavarjan Branch , Rezvani Sichani ، Ziba Department of Biochemistry - Faculty Biology - Islamic Azad University, Falavarjan Branch , Rezvani Sichani ، Adel Department of Food Science and Technology - Islamic Azad University, Shahreza Branch , Nayeri ، Hashem Department of Biochemistry - Faculty Biology - Islamic Azad University, Falavarjan Branch
From page
26
To page
29
Abstract
Background: Cancer metastasis is the leading cause of death among cancer patients, but there are numerous treatment options available, including drugs such as albendazole (ABZ) and complementary therapies such as cannabis-based medicines, making them important targets for therapeutic interventions. The present study aimed to assess the impact of ABZ on the protein expression of Tau and Stathmin, as well as cell migration, in patients with metastatic breast cancer (BC), where these proteins play critical roles. Materials and Methods: MCF-7 and MDA-MB-231 cell lines were split into a treatment group that received varying concentrations of a standardized extract of ABZ for 48 hours and a control group that received no treatment in this study. The relative gene expression was measured using a quantitative reverse transcription-real-time polymerase chain reaction assay and the ΔΔct method. A migration assay was also performed to assess cancer metastasis. Results: Tau and Stathmin gene expression and cell migration were significantly decreased compared to the control group. Conclusion: The results of the study demonstrated that ABZ reduced both Tau and Stathmin gene expression, as well as cancer metastasis. Nonetheless, evidence suggests that we can use ABZ as an anti-tumor drug for BC treatment.
Keywords
Metastasis , Albendazole , Tau , Stathmin , Breast cancer
Journal title
Disease and Diagnosis
Journal title
Disease and Diagnosis
Record number
2758997
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